Gas extractor and injector for gas chromatography



vS. NATELSON Oct. 29, 1968 GAS EXTRACTOR AND INJECTOR FOR GAS CHROMATOGRAPHY 7 Sheets-Sheet 1 Filed June 2l, 1963 mz m2@ @J @203m mf @E Oct. 29, 1968 s. NATELsoN 3,408,166

GAS 'EXTRACTOR AND INJECTOR FOR GAS CHROMATOGRAPHY Filed June 21, 1963 7 sheets-sheet 2 78 DRYiNG AGQNTS TANK OF HEUUM RYDROUS 2O C3504 a@ GAS CHROM- GAS VENT /75 ffm RECORDER L SAMUEL NATELS INVENTOR, ON

attorney S. NATELSON Oct. 29, 1968 GAS EXTRACTOR AND INJECTOR FOR GAS CHROMATOGRAPHY FiledJune 21. 1963 7 Sheets-Sheet 3 fil l SAMUEL NATELSON attorney S. NATELsoN Oct. 29, 1968 GAS EXTRACTOR AND INJECTOR FOR GAS CHROMATOGRAPHY Filed June 2l, 1963 7 Sheets-Sheet 4 FIGB SAMUEL NATeLsoN mvsmon attorney S. NATELSON Oct. 29, 1968 GAS EXTRACTOR AND INJECTOR FOR GAS CHROMATOGRAPHY 7 Sheets-Sheet 5 Filed June 21, 1963 SAMUEL NATELSN n INVENTOR.

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attorney Oct. 29, 1968 s. NATELsoN 3,48155 GAS EXTRACTOR AND INJECTOR FOR GAS CHROIIATOGRAPHY Find June 21, 1963 '7 sheets-sheet e rrOQ/VEY S. NATELSON Cet. 29, 1968 GAS EXTRACTOR AND INJECTOR FOR GAS CHROMATOGRAPHY 7 Sheets-Sheet 7 Filed June 21 1965 arroA/.EY

United States Patent O 3,408,166 GAS EXTRACTOR AND INJECTOR FOR GAS CHROMATOGRAPHY Samuel Natelson, Valley Stream, N.Y., assignor to Scientific Industries, Inc., Queens Village, N.Y. Continuation-in-part of application Ser. No. 221,172, Sept. 4, 1962. This application June 21, 1963, Ser. N o. 289,680

2 Claims. (Cl. Zit-253) ABSTRACT F THE DISCLOSURE A device for the chromatographic analysis of components in trace amounts of volatile substances in a mixture, which includes means to eliminate a change in a recorder baseline due to different rates of carrier gas ow, comprising an adjustable bypass whereby the gas flow impedance of a sample chamber may be matched with that of the bypass.

This application is a continuation-in-part of my United States patent application Ser. No. 221,172 filed Sept. 4, 1962, and since issued as United States Patent 3,171,722 on Mar. 2, 1965.

The present invention relates to an instrument for the accurate sampling of gases or liquids for the purpose of injecting them into a flowing gas stream of an inert gas such as argon or helium which will carry the sample to a gas chromatography instrument usually having a column designed for the separation of the sample into its components parts and a detector for detecting and assaying the components as they leave the column.

Gas chromatography is a widely used technique for determining the components of a mixture. Present practice consists of sampling a small volume of material (eg. 1 to 100 microliters) into a syringe. The needle of the syringe is sharp and narrow so that the sample can be injected through a rubber dam into the stream of a flowing inert gas. The gas carries the sample to a column for separation. This column can be a narrow capillary or an inert supporting medium which is coated with a lm of non-volatile oil. The components of the sample now are progressively dissolved and eluted from the nonvolatile oil. Since gases, such as propane and butane, would have different solubility and eluion rates from the oil, they gradually separate. As they leave the column, the different fractions are detected by a variety of procedures such as ditferences in thermal conductivity from the inert carrying gas, effect on the conductivity of a ame when burned, conductivity of ions formed when activated by a radioactive substance such as tritium or strontium -90 and a variety of other procedures.

In the case of gases ilke oxygen, nitrogen and carbon dioxide, the column may contain no oil but contain a granular material such as natural or synthetic aluminum silicates or silica gel. In this case, the gases diffuse into the pores of the material and diffuse out sequentially. Thus, in effect the porous material serves to separate the gases such as oxygen and nitrogen by their different rate of diffusion into and out of the porous substances. Eventually, the gases separate and can be detected by various techniques, usually thermal conductivity. It is apparent that in this technique of gas chromatography, the column needs to be tailored to tit the needs of they substances to be separated. A column which is satisfactory for gasoline mixtures may not serve for separating the components of ordinary air. n

At times, the problem is to analyze a small amount of volatile substance dissolved or suspended in a relatively large volume of solvent. Such a problem exists when one p 3,408,166 Ice Patented oct. 29, 1968 wishes to analyze for the oxygen, nitrogen, carbon monoxide, or carbon dioxide content of blood. Another similar problem is the analysis of anethesia volatiles, e.g., nitrous oxide dissolved in blood. Still another such problem is the analysis for air, i.e., oxygen and nitrogen dissolved in kerosene or jet fuel. Yet another such problem exists when one Wishes to analyze for poisonous volatiles in blood such as carbon monoxide, methanol, chloroform, hydrogen cyanide and other poisons inhaled accidentally.

While gas chromatography has been extensively studied for these purposes, the technique has not been successful fore accurate quantitative analysis because of certain difficulties with the conventional methods. One cannot inject blood, for example, directly into the ow of inert gas because it would rapidly foul the columns. Thus, it becomes necessary to separate the blood from the gases. The known techniques can be divided into two general classes, neither of which is satisfactory. In one procedure, the inert gas flows into and out of a little bottle or chamber. To take a specific example, the analysis of blood for oxygen, nitrogen and carbon dioxide, the chamber contains dilute sulfuric acid. Since the water in this solution is constantly evaporating it is necessary to provide a column of drying agent which fouls quickly with the large amount of water being evaporated. The blood is sampled in a syringe. This is at best only an approximate measuring technique. The blood is now injected through a rubber dam into the little bottle. The acid liberates the carbon dioxide, and ferricyanide solution in the bottle liberates the oxygen. The nitrogen is also liberated by diffusion into the inert gas such as helium. The gases, particularly oxygen held by hemoglobin are liberated slowly. Thus, this gas is fed to the column in decreasing amounts over a relatively long period of time. When the gas comes olf the column and the signal is translated by the recorder, a peak is observed which trails off gradually. This phenomenon is known as trailing. Ideally a symmetrical curve should be drawn. The trailing curve is difficult to quantitate and one has to estimate the area under the curve by approximate methods.

In order to avoid the phenomenon of trailing some scientists use a bypass. In this technique, the gas is allowed to ow through the little bottle. lBefore injecting the sample, the bottle is cut off from the main stream of helium by two valves permitting the helium to ow through a bypass to the columns. After injection and after the oxygen and other gases have been completely liberated, the valves are turned permitting the gases to be swept into the column. This technique can introduce serious error. The flow of helium must not be disturbed or false patterns will be obtained. With this technique the path is changed, the gas resistances are different when the stream is through the bypass from what it is when gas flow is through the bottle. This is evident on the gas chromatograph recorder by a change in baseline which does not return to normal until long after the curves have been drawn. The curves drawn are thus only an approximation of what they should be since to those skilled in the art of gas chromatography it is essential that the path of the gas remain constant, with constant rate and constant gas resistance. Although many attempts may have been made to solve the foregoing and other difficulties, none, as far as I am aware have ever been successful when carried out into practice.

-The present invention describes a system which avoids the foregoing dithculties and a constant baseline is obtained. Curves drawn are so smooth and symmetrical, and reproducible that after proper standards are rst run, it is no longer necessary to measure the area under the curves but peak heights may be used for accurate analysis, although highest precision of course requires that the area under the curves be measured, even under ideal conditions. Furthermore, in the present system, only a small amount of drying agent, such as anhydrous calcium sulfate need be used since the liquid does not evaporate into the columns. This is achieved by injecting only the liberated gases into the column by means herein described. Since the gases injected contain water vapor, it is preferable to remove the water vapor from them by a drying agent. But when the water vapor is being measured, as in kerosene, the drying agent is omitted so that the Water vapor will be separated on the columns. In this case, the water vapor is treated as a gas to be assayed.

Thus, an object of the present invention is to provide an arrangement for the separation of gases and liquids so that the gases may then be analyzed by gas chromatography. l

Another object of the present invention is to provide an arrangement for feeding precise quantities of gases to a gas chromatography device.

Still another object of the present invention is to provide an arrangement whereby very small quantities of gas may be analyzed by gas chromatography, either using a free flowing inert gas or by injecting the inert gas with the gas chromatography device as a single plug.

Yet another object of the present invention is to provide an arrangement which will provide samples in consistent quantity and volume so that consistent results are obtainable on the reading means of a gas chromatography device Without incorrect initial peaks and trailing readings at the ends of recorded curves.

With the foregoing and other objects in view, the invention resides in the novel arrangement and combination of parts, in the details of construction, and in the process steps hereinafter described and claimed, it being understood that changes in the precise embodiment of the invention herein disclosed may be made within the scope of what is claimed without departing from the spirit of the invention.

The invention will appear more'clearly from the following detailed description when taken in connection with the accompanying drawing, showing by way of example, preferred embodiments of the inventive idea.

FIGURE la is a block diagram of the instrument contemplated herein;

FIGURE 1b is a perspective and partially schematic view of the instrument contemplated herein;

FIGURE 2a depicts a longitudinal cross-sectional view of a portion of a driving arrangement contemplated here- 1H;

FIGURE 2b illustrates in perspective one of the cornponents shown in FIGURE 2a;

FIGURE 2c illustrates in perspective another component shown in FIGURE 2a;

FIGURE 3 shows a more detailed view of still another component arrangement shown in FIGURE la;

FIGURE 4 shows in detail yet another perspective view of a component illustrated in FIGURE la;

FIGURE 5 illustrates an arrangement for coupling the present invention to a gas chromatograph instrument so as to provide slug delivery;

lFIGURE 6 depicts another arrangement for coupling the present invention to a gas chromatograph instrument so as to provide improved slug delivery; and

FIGURE 7 shows a preferred arrangement for coupling the present invention to a gas chromatograph instrument so as to provide the improved slug delivery described in FIGURE 6.

Generally speaking, the instrument will include a uid sample input conveying zone 11 for conveying a uid sample 12 to be tested to a liquid-gas separation zone 13 having separation means 14 therein for liberating gases from liquids. After the gases have been liberated from the liquids, the liquids are carried to a liquid storage zone 15.

This movement of the uid sample is driven by a drive- 4. fluid in a chamber 16, e.g., mercury, controlled by the action of driving means 17. When the liquid part of the sample has been removed from the separation zone 13 into liquid storage zone 15, the drive fluid will drive the gas in the separation zone to the output conveying zone 18, drive fluid moving through a drive iluid bypass lzone 19. From the output conveying zone 18, the gas is sent to a gas chromatograph instrument 20, either by Ainjection of the gas to be analyzed into a free owing inert carrier gas or by mixing the gas to be analyzed with a small portion of the carrier gas and lthen directing this mixture to the columns in the form of a single slug. A first gate means 21 will permit the sample to pass either from input conveying zone 12 to the liquid-gas separation zone 13 or permit gas in the separation zone 13 to go to the output conveying zone 18. A second gate means 22 will permit liquid to go from the liquid-gas separation zone 13 into the liquid storage zone 15 or some drive fluid to go from the drive uid bypass zone 19 into the liquid-gas separaltion zone 13 to force the gas therein into the output conveying zone.

In carrying the invention into practice, the instrument is iirst filled with mercury and the sample 12 to be analyzed is introduced into the input conveying zone 11 of the instru-ment or pipet 30 having a bent tube 31 of relatively large outside diameter and a capillary end bore 32 drawn to a fine or minute opening, and calibrated at .01, .02 and .03 ml. with calibration marks 33, measuring in this case to 0.01 ml. A ball joint 34 couples the inner end 35 of bent tube 31, to rst gate means 21, namely a first two-way stop cock 38. When the stop cock is at the 0 position, stop cock 38 couples inner end 35 of the bent tube to the liquid-gas separation zone 13. When the stop cock is at the position, the liquid-gas separation zone is sealed off, and when at the position, the stop cock couples the liquid-gas separation zone to the output conveying zone 18.

Liquid-gas separation zone 13 includes a separation or reaction chamber 39 having a hemispherical portion 46 and a flattened wall portion 47 with a depression 48 therein. Reaction chamber 39 is acted upon by separating means 14 which includes spinner 49 made froml iron, alnico, cobalt platinum alloy or other substance capable of being magnetized within the reaction chamber 39, spinning alnico magnet means 44 to turn the spinner, and a motor 45 to turn the magnet means. The spinner is preferably covered with Teon or glass to protect the glass wall. When the reaction chamber is sealed oiI and spinner 49 turns, the gas will be liberated from the sample in the reactionchamber. Below the reaction chamber 39 is a liquid storage zone 15 having a reservoir 40 therein and a mercury bypass line 19 in parallel therewith. Interposed between reservoir 40 and parallel mercury bypass line 19 on the one hand and reaction chamber 39 on the other hand is a second two-way stop cock 41 similar to stop cock 38 so that at 0 position the reservoir 40 is coupled to the reaction chamber 39; at 90 position, the reaction chamber is sealed oi from both the reservoir andy bypass line 19; while at the 180 position, the bypass line is coupled to the reaction chamber. Reservoir 40 and mercury bypass line 19 are coupled' to a common junction 42 having a ball joint 43 rconnecting common junction 42 to the container of drive iiuid 16, and its associated driving means 17 This portion of the instrument includes a barrel 51 for the drive Huid, an opening 52 in the upper part of the barrel and a connection to ball joint 43 and a stainless steel or glass plunger or piston 53 in the barrel. The

' barrel 51 is preferably of glass, sealed at one end and ground at at the other end. The piston moves forward and backwards in the barrel to displace the drive uid usually mercury although other non-volatile liquidssuch as silicone Oils may be used. The piston 53 enters the barseal fits close to the fbarrel and has annular rings eut'into it to make it more liexible and to permit the barrel to slide smoothly in and out over the seal up to a flange 54a on the seal having a at surface so that when the end of the barrel is pushed against it a seal is made. Over the sealed end of the barrel is a tapered screw cap 55 with a hole 55a designed to engage tapered threads 5411 on seal 54. The outer end of the barrel also includes a tightening screw 56 designed to force the barrel 51 and the ground end thereof against liat surface of llange 54a to seal it.

The barrel and piston arrangement is held in place by an assembly of supporting members. Thus, tightening screw 56 is held rigid by rst transverse support 57 which in turn is connected to longitudinal tie rods 58a and SSb by set screws 59. Seal 54 is held by second transverse support 60 also coupled to tie rods 58a and 58h while piston 53 is supported outside of the barrel by third transverse support 61, this transverse support unlike the others glides over or along tie rods 58a and 58b according to the movement of the piston 53 in and out of the barrel. Piston 53 has a flanged end 62 held to third transverse support 61 by a set screw 62a acting on a rubber washer 63. Third transverse support 61 and piston 53 are moved by a threaded rod 64 which moves into the hollow of the piston as drive Wheel 65 is rotated. This serves to balance support 61. When drive wheel 65 is turned one way, piston 53 advance into the barrel while drive Wheel 65 is turned the other way, the piston moves out of the barrel. ln this way the mercury drive fluid is raised or lowered in the upper part of the instrument. To facilitate the gliding of support 61 along tie rods 58a and 5817, bearings 66 are provided. To support threaded rod 64, a fourth transverse support 67 having a bearing 68 is provided, While to turn wheel 65 by hand, a handle 69 is provided. For motor drive of threaded rod 64 there is a pulley 70 driven by a belt 71 and a motor 72.

Advantageously, the instrument may have a manometer likewise coupled to the barrel 51 at opening 52 through the leg of a Y-tube 73, one arm of the Y-tube having a ball joint 43 being coupled to the junction of the reaction chamber and the bypass line, the other arm of the Y being coupled to the manometer 75 -by a ball joint 74. The manometer will have uniform markings 76 in millimeters so that the pressure can be measured. Manometer 75 also has a reservoir 77 to hold the overflow of mercury by means of a stopcock 78 at the top of the manometer, and will also include a safety bulb 79 to prevent pulling the mercury down too low.

Returning now to the reaction chamber 39 in liquidgas separation zone 13 and two-way stopcock 38 acting as first gate means 21, after the liquid and gases have been separated, it is necessary to send the gas from the liquid-gas separation zone 13 into the gas chromatograph instrument through output conveying zone 18. To this end, second two-way stopcock 41, when turned to the 180 position previously mentioned will couple the mercury bypass line 19 to the reaction chamber 39. At the same time, by turning rst stopcock 38 to the 180 position, reaction chamber 39 is coupled to the output conveying zone 18. It is at once apparent that by pushing piston 53 into barrel 51, the mercury drive iluid is forced along bypass line 19 into the reaction chamber, forcing the gas therein through stopcock 38 into the output conveying zone 18. This portion of the instrument is coupled to stopcock 38 across a ball joint 80 and includes a narrow capillary tube 81 of the order of 0.3 mm. bore to prevent gas dilusion. The tip 82 of this narrow capillary discharges into a gas iiow chamber 83 disposed at right angles to capillary tube 81 and having an inlet tube 84 to permit the helium or other inert gases to enter. Disposed over tip 82 of the capillary tube is a platinum wire 85 for making electrical contact. This wire is about l mm. distance from the tip and when mercury emerges from the capillary, it closes the Contact stopping the motor driving the mercury upwards to inject the gas.

At the end of the gas ow chamber opposite inlet tube 84 is outlet tube 86 to the gas chromatograph. Towards this end of the chamber there will also be a stopcock 87 on a drain 88 for draining the gas ow chamber of any liquid which may get into it. In some cases, additional tubing such as connecting elbow tube 89 from the gas tank to the gas oW chamber may be required.

To operate the instrument, the instrument is irst lled with mercury to tip 32 of pipet 30 and to the tip of injector, i.e., tip 82. Stopcock 38 is turned so 'as to connect reaction chamber 39 to pipet 30. Stopcock 41 is turned so 4as to connect reservoir 40 with reaction chamber 39. The inert gas, e.g., helium is flowing steadily into and out of gas flow chamber 83 into a chromatograph connected to a recorder. Wheel is turned counterclockwise while pipet 30 dips into blood. A quantity of 0.03 ml. is sampled. This is followed by taking up some mercury, about 0.01 ml. Then, a reagent desi-gned to liberate oxygen, e.g., ferricyanide reagent, is taken up. Mercury is now `again taken up until the blood and the reagent are brought below stopcock 38. Stopcock 38 is now turned 90 so that the sarnple and reagent are isolated from the helium or air. Motor 72 is started by pressing -a button so that the mercury is lowered to create a vacuum. The mixture of the blood and reagent is brought to the bottom of the reaction chamber 39. Motor 45 is started and spinner 49 spins to mix blood and the reagent until all the gases have been liberated. The sample is now ready to be injected in the gas chromatography device. As will be explained hereafter, the manometer, if the instrument has one, can be used to check to see if all the gases are liberated. After the gases have been liberated, the piston or plunger is pulled back until the liquid mixture o-f blood and reagent is in the reservoir 40, the liquid -meniscus being just below reaction chamber 39. Now, only gas is in the reaction chamber. Stopcock 41 is now turned from the 0 position to the 180 position to connect with ythe mercury in mercury bypass line 19 which is now brought up with motor 72 to the 0.12 mark 39a in the reaction chamber 39. The gases are now under la partial vacuum ready to be injected. At this point, stopcock 38 is Aturned 90 to the 180 position so as to connect reaction chamber 39 to gas ow chamber 83. The helium pressure which `is above atmospheric pressure will cause the mercury extending from stopcock 38 up to tip 82 to be pushed back into the reaction chamber. When this has settled down, motor 72 is started. The mercury rises and ejects the gas into the gas stream at `a constant rate, rapidly. When the meniscus of the liquid or mercury reaches the tip 82 -it makes contact `with platinum wire land stops the motor. This action of the mercury in stopping the motor by contacting the platinum wire 85 is that of the well known mercury switch land for this reason the feedback circuit to stop the motor is not shown in the drawing.

Thus, the gases are injected in exactly the same way each time to get reproducible curves on the recorder of the chromatograph. While the pattern is developing on the recorder 20a, stopcock 38 is turned again to the 0 position to connect the pipet 30 .again to reaction chamber 39. The mercury is lowered so that the meniscus is at the bottom of the reaction chamber 39. Stopcock 41 is now turned another to the 0 position to connect reservoir 40 with the reaction chamber 39 by advancing the mercury with motor 72 or hand wheel 65 so that this set of components move the piston into the barrel. The blood and reagent float above the mercury and are ejected from the instrument through pipet 30. Wash liquids such as water and detergent are then brought into the machine so as to wash the instrument clean of the Iprevious sample and then these are again ejected through the pipet. The mercury is now brought to the tip of the pipet and the process of lanalysis can now be repeated.

Since stopcock 38 can be turned so that reaction chamber 39 is connected to the pipet independently of the connection to the chromatograph, the pattern on recorder 20a can be developingl while the gas from the next sample is being extracted. As soon as the pattern has been recorded or read, the next gas sample can be injected in the gas chromatograph apparatus immediately. From the foregoing it is -apparent therefore that the calibrated pipet assures precise sample measurement and the operating eiciency is limited only by the speed of the developing chromatogram because while the chromatogram is developing, the next sample is prepared for injection. Furthermore, the instrument can be used for injecting into any gas chromatograph apparatus and can be used for routine determinations and special problems. Although not essential to many determinations, the manometer is useful as a check to see if all the gases are liberated. This is accomplished by rst raising the meniscus of the mercury to the 0.12 mark 39a and recording the pressure in the manometer as the height of the mercury therein. After the gases have been liberated, the mercury is again brought up to the 0.12 mark 39a and the reading in the manometer should be the same as before. This mercury height is also a -measure of the volume of the mixed gases liberated and is of value when this information is needed.

The present invention is especially useful with existing equipment. In this connection, slug delivery of the sample has certain advantages when injecting the gas into small narrow columns. All the gas to be separated reaches the columns simultaneously which aids in obtaining sharper separations. As hereinbefore mentioned, there is a tendency for the base line to change when using slug delivery because one must go from sample to bypass, thus changing the pressure in the tubes. In addition, slug delivery is particularly useful for the purpose of programming the instrument. When the quantity of a particular gas in the sample is extremely small the gas chromatograph can be programmed so that low sensitivity is used when abundant gases are being detected and high sensitivity is used when the smaller component is going through the detector. To do this effectively all the gases should reach the first column simultaneously.

There is shown in FIGURE how, lacking other equipment, the invention herein contemplated can be used with a commercially available arrangement or third gate means for slug delivery. Here we have a gas ow chamber 83a coupled to a source of inert gas in parallel with a gas bypass line 101. Gas flow chamber 83a has bottom configuration to permit mercury to ow back into the capillary tube, which does not project into the chamber. Many of the commercially available gas chromatograph instruments are equipped with a four-way valve 102, which can be used as the third gate means. This valve permits switching from one flow system to another or to gas bypass as shown by the broken lines, the solid line indicating one valve position, the broken line indicating another valve position. When the gas chromatograph being used has such a valve, or when only such a valve is available locally for attachment to the gas chromatograph instrument, the instrument of the present invention may be used for slug delivery. In this case, just before injecting the released gas into the gas flow chamber, the four-way valve 102 is turned to gas by-pass. The mercury is then raised to drive the sample into the gas ow chamber 83a which is now isolated from the system. In this way the gas flow chamber now contains helium plus the injected sample gas at only a slightly increased pressure. This is so because the volume of the gas flow chamber, even when small (of the order of 0.5 to 1.0 mL), is usually many times larger than that of the sample which is of the order of 0.015 ml. at standard conditions. Thus, with the gas ow chamber of 0.5 ml. in size the increase in pressure will be 515 divided by 500 of the original pressure. Thus, the original pressure is increased by approximately 3%. If the initial volume of the gas flow is greater than 0.5 ml. this increase in pressure will be even smaller. When, vas shown in the drawing the valve passage as shown by the solid lines are connected across the gas bypass, and, at this point, valve 102 is turned in the way shown by the broken line, all the gas in the gas flow chamber 83a is swept in one slug into the gas chromatograph instrument. For very small volumes of gas this will tend to produce very sharp peaks. Thus, when used with an instrument equipped with a four-way valve, the helium stream from the inert gas tank is split into two branches. One branch goes to the four-way valve, the other to the gas ow chamber. Thus, two distinct gas paths are used: when the four-way valve is turned to gas by-pass; and, when turned to gas ow chamber. Unfortunately, this arrangement suters from the defect that the two paths are not identical because the path from the gas flow chamber includes a water desiccant or drying agent. This causes the path through the flow chamber to have a relatively high resistance to the gas by-pass line. If the gas by-pass line is also fitted with a desiccant tube, it does not solve the problem because the amount of moisture from the sample is dierent from the moisture obtained from the helium alone. Moisture in a drying tube tends to change its resistance. Thus, the flow chamber path resistance is a variable from run to run while the by-pass path remains essentially constant.

This difference may be corrected `by using the arrangement shown in FIGURE 6. Here is shown capillary tube 81 with its tip 82 coupled to gas-dow chamber 83a. This is the chamber with the bottom conguration which permits the mercury to fall back into the capillary when pressure is released. In this gas ow chamber, the capillary tube does not project into the chamber. In parallel with chamber 83a is a gas by-pass line 101g, with an adjustable section 103. On both sides of the by-pass line 101a and gas ow chamber 83a are two-way stop cocks 104 and 105. When the two stop cocks are simultaneously turned one way, the path is through the gas by-pass line; when simultaneously turned the other way, the path is through the gas How chamber. The resistance of the adjustable portion 103 of the by-pass line can then be readily adjusted to that of the gas flow chamber. But, the simultaneous turning of the two stop cocks is of course a nuisance. A preferred arrangement is shown in FIGURE 7 wherein there is shown a preferred form of third gate means, i.e., a double two-way stop cock 106. Depending on the position of the double two-way stop cock the inert gas will either ow through stop cock channel 101b along gas bypass line 101C: to stop-cock channel 101C and to the gas chromatograph device; or the gas flows from the source through stop-cock channel 83h across the gas ow chamber 83a, through stop-cock channel 83C to the gas chromatograph device. Again, there is an adjustable section 103 to equalize changes in the resistance of the gas flow channel. This arrangement as well. as the arrangement of FIGURE 6 permits efcient slug delivery into the gas chromatograph device with a fairly constant base line. This is because of the fact that the drying agent is interposed between the gas chromatograph device on the one side and the outflow line coming from the by-pass line and the gas ow tube.

For the purpose of giving those skilled in the art a better understanding and appreciation of the invention, the following illustrative examples are given:

Example 1 between two layers of mercury. The tip is wiped and dipped in a reagent made up of l gram potassium ferricyanide dissolved in ml. of 0.8% saponin solution. A layer of caprylic alcohol covers this solution to exclude air. Before use the reagent is de-aerated by evacuation. 0.01 ml. of caprylic alcohol followed by 0.2 ml. of the ferricyanide reagent followed by 0.01 ml. of caprylic alcohol is drawn up in that order. The tip lis wiped and now dipped in mercury. Mercury is drawn beyond the 'first gate means stopcock so as to sweep the blood and reagents into the reaction chamber. The first stopcock is closed.

The piston is now retreated to create a vacuum and bring the reagents into the reaction chamber. The spinner is started to mix the reagents and aid in the liberation of the gases. After three minutes the piston is retreated to bring the mercury and all of the solution into the liquid storage zone. The second gate means stopcock is turned 180 and the piston brought forward to bring mercury to the reaction chamber through the bypass line. The gases are now in the reaction chamber. The first gate means stopcock is now turned so that the chamber communicates with the flowing helium stream. Any mercury above the stopcock on the flow chamber side is driven into the chamber by the pressure of the helium. 'I'he motor is started. This drives the gases upward into the iiowing helium stream. When the mercury protrudes so as to make contact with the tip of the contact needle in the fiow chamber, the motor stops. 'Ihe first gate means stopcock is now turned 180. The mercury in the chamber, above the second gate means stopcock is lowered with the piston until it is just above this second stopcock. The second stopcock is now turned 180 and the reagents and spent blood held in the storage zone is ejected and discarded. After rinsing the machine twice with water. by bringing the water in and ejecting by means of the piston, the instrument is ready for the next sample. The gas chromatograph draws the gas pattern while the next sample is being processed.

Example 2 For the analysis of dissolved gases in jet fuel the procedure of Example 1 is followed with the following changes:

0.2 ml. of jet fuel is sampled by the pipet as before. For convenience the jet fuel is poured into a test tube containing mercury. The pipet with a bubble of mercury protruding from the tip is dipped into the jet fuel. 0.2 ml. is sampled by retreating with the piston. Without removing the tip from the jet fuel it is dipped directly into the mercury at the bottom. The mercury is now drawn in to sweep the jet fuel into the reaction chamber. The first stopcock is turned 90 to close. The piston is retreated to evacuate the gases the upper meniscus of the jet fuel extending into the reaction chamber. The spinner is started to mix the jet fuel so as to assist in the liberation of the gases. After three minutes the jet fuel is sequestered in the storage zone as in Example 1 and the liberated gases injected into the helium stream as in Example 1. The gas pattern now is drawn on the gas chromatography recorder.

Example 3 Using the apparatus of FIGURE 7, the technique of Example l is used to extract the gases. Just before the first gate means is turned to inject the gas into the gas flow chamber, the stopcock of the ow change is turned so that the carrier gas goes through the gas by-pass. At this point first gate means is opened. The mercury above this stopcock on the ow chamber side lis driven down into the reaction chamber by the pressure of the helium. At this point the piston is advanced so as to drive the liberated gases and the helium which has entered the reaction chamber into the now isolated gas ow chamber. First gate means is turned 180. The stopcock of the flow chamber is now turned 180 so as to permit the inert gas to ow through the ow chamber and sweep the gases, in one slug, into the gas chromatograph. By this procedure extremely sharp peaks are recorded.

It is to be observed therefore that the present invention is directed to an instrument for liberating volatile material in a sample mixture 12 of volatile and non-volatile material and injecting the volatile material into a gas chromatograph apparatus. The instrument comprises the combination of an input zone 11 for taking up the sample; a separation zone 13 coupled to the input zone, including separation means 14 therein; a storage zone 15 for temporarily storing a liquid therein; a drive Ifluid chamber 16 coupled to said storage zone designed to hold a drive fluid therein including lfluid driving means coupled to said chamber; a drive iiuid bypass zone 19 in parallel with said storage zone between said separation zone and said chamber; an output conveying zone 18 coupled to said separation zone; and, first and second or gate means 21 and 22, connecting in the first instance said separation zone and either said input or output zones, and in the second instance said separation zone and either said storage or bypass zones, or the gate means block the couplings to all of said zones. The first and second gate means are shown as two-way stopcocks 38 and 41 having three positions. The storage zone and bypass zone are connected to two arms of a three-way connector. The drive liuid chamber which is connected to the third arm of the connector is barrel-shaped and the driving means includes a piston disposed for axial movement in the barrel. The output conveying zone includes a narrow capillary 81 with a tip. The capillary #is coupled to said first gate means discharging into a gas flow 83 disposed transverse to the capillary. In the vicinity of tip 82 is a contact 85 designed to be part of electrical circuitry to close the fluid drive means 17 when the drive fluid passes through the tip and touches the contact.

Preferably, the volatile material in the sample mixture is injected into the output conveying zone while a steady stream of inert gas, e.g., helium is flowing therethrough. However, when the volume of the volatile sample material is very small, slug delivery of the sample into the gas chromatograph instrument will provide amplification or sharp peaks which will assist in reading the results. If the gas chromatograph instrument is equipped with a four-way valve, gas from the inert gas source may be directed on the one hand through the gas flow chamber and on the other hand through a gas by-pass line. Before injecting the sample into the gas flow chamber, the four way valve is first turned to gas by-pass. After the sample is injected into the chamber, the four-way valve is turned to sweep the sample from the chamber through the gas chromatograph instrument. A double two-way stop cock may advantageously be used. In one position of the double two-way stop cock, the path of the inert gas is from the inert gas source, through a first channel in the stop cock along the gas by-pass to a third channel in the stop cock and out towards the gas chromatograph instrument. In a second position, the inert gas flows from the inert gas source through a second channel in the stop cock through the gas ow chamber containing the sarnple, to a fourth channel in the stop cock and from there to the gas chromatograph instrument. The preferred arrangement has the advantage that the resistance through the gas ow chamber containing the sample can be equalized by an adjustable portion in the gas by-pass line and a drying agent if used can be interposed between the double two way stop cock and the gas chromatograph instrument.

Thus flow from the by-pass or the flow chamber both go through the same drying tube.

It will be apparent to those skilled in the art, that my present invention is not limited to the specific details described above and shown in the drawing, and that various modifications are possible in carrying out the features of the invention and the operation and method of support, mounting and utilization thereof, without departing from the spirit and scope of the appended claims.

I claim:

1. In a device for the analysis of components in trace amounts of volatile substances in a mixture, which includes: a separation chamber, means for separation of the trace amounts of volatile components from the mixture, and means for injecting said trace amounts into a gas chromatograph, and wherein, the means for the separation of the trace amounts of volatile components of the mixture comprise, a calibrated pipet for sampling the mixture, said pipet communicating to the proximal end of a separation chamber through one upper end of an upper two-way stop cock, a gas flow chamber, the other upper end of said stop cock communicating with said gas How chamber; a piston inserted into a barrel filled with mercury communicating with the distal end of the separation chamber so that when the piston is withdrawn the sample is made to move beyond the upper two-way stop cock into the separation chamber and when said stop cock is closed and the piston is withdrawn further, a vacuum is created causing the trace amounts of the volatile components to volatilize from the mixture; a lower two-way stop cock disposed between the barrel and the separation chamber, said lower stop cock having one leg on its upper side connecting said stop cock with said separation chamber and two legs on its lower side and a storage chamber in one lower leg so that non-volatile liquid components of the mixture may be drawn below the lower two-way stop cock, leaving the volatile components in the separation chamber, and when the lower two-way stop cock is turned 180 permitting an alternate communication path between the barrel and piston combination with the separation chamber, thus permitting, by |advancing the piston, the injection of only the volatiles into the gas flow chamber, the improvement which comprises:- conduit means connecting both ends of said -gas ow chamber to a iirst and second double stop cock, the first double stop cock communicating to a source of carrier ow gas through a lirst t-ube and the second double stop cock communicating to a gas chromatograph through a second tube; an adjustable by-pass line disposed parallel to the gas ow chamber and connected between the first and second double stop cocks for varying the impedance of the ow of the carrier gas through said by-pass so that the ow of said gas can be made equal to the flow of gas through said gas flow chamber, and hence, when the -rst and second double stop cocks are turned at 180 the carrier gas may flow alternately either through said gas ow chamber or through the by-pass line at the same rate, the trace volatile components being injected into the gas chromatograph as a slug of gas without disturbing the pattern obtained on the chromatogram due to change of flow rate when the sample is injected said gas ow chamber being of a conguration such that any liquid carried into said chamber drains from a lowest point in the bottom thereof.

2. An instru-ment as claimed in claim 1, said flirst and second stop cocks being combined into one conical unit with inner and outer sections having one and the other sides, with three inlets on each of said sides on said outer section and pairs of passages serving said inlets across said inner section, said inner section being rotatable so that pairs of inlets on the one side can be selectively connected 'with diterent pairs of inlets on the other side by the rotation of said inner section.

References Cited UNITED STATES PATENTS 2,206,816 7/ 1940 Levitt 23-292 2,680,060 6/ 1954 Natelson 23-253 3,096,157 7/ 1963 Brown et al. 23-232 3,171,722 3/ 1965 Natelson 2.3-253 2,449,067 9/ 1948 Guillemin 23-254 OTHER REFERENCES Desty, D. H., Editor, Gas Chromatography 1958, Butterworths Scientific Publications, London (1958), pp. 28B-293, POSL Call No. QD 271, I5.

MORRIS O. WOLK, Primary Examiner.

R. E. SERWIN, Assistant Examiner. 

